US4479985A - Method for cleaning and clearing plastic surfaces - Google Patents

Method for cleaning and clearing plastic surfaces Download PDF

Info

Publication number
US4479985A
US4479985A US06/331,489 US33148981A US4479985A US 4479985 A US4479985 A US 4479985A US 33148981 A US33148981 A US 33148981A US 4479985 A US4479985 A US 4479985A
Authority
US
United States
Prior art keywords
formulation
cleaning
resin
coating
alkyd
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US06/331,489
Inventor
Jefferson K. Allen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US06/331,489 priority Critical patent/US4479985A/en
Application granted granted Critical
Priority to US06/666,563 priority patent/US4595719A/en
Publication of US4479985A publication Critical patent/US4479985A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/0427Coating with only one layer of a composition containing a polymer binder
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/043Improving the adhesiveness of the coatings per se, e.g. forming primers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/046Forming abrasion-resistant coatings; Forming surface-hardening coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/06Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2333/10Homopolymers or copolymers of methacrylic acid esters
    • C08J2333/12Homopolymers or copolymers of methyl methacrylate
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31924Including polyene monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31928Ester, halide or nitrile of addition polymer

Definitions

  • This invention relates to a method and composition for cleaning and preserving in a clear condition transparent plastic sheets for example, windows, such as "PLEXIGLAS".
  • U.S. Pat. Nos. 3,904,732 and 3,677,821 are broadly directed to restoring the surfaces of plastic sheets such as "LUCITE” and “PLEXIGLAS", polymethylmethacrylates.
  • My invention is more particularly directed to overcoming the problems associated with so-called plastic or synthetic transparent windows such as those windows formulated primarily or entirely from methylmethacrylate.
  • my invention comprises cleaning a surface of a transparent methylmethacrylate (a thermoplastic poly-type polymer more specifically an acrylic monomer).
  • a transparent methylmethacrylate a thermoplastic poly-type polymer more specifically an acrylic monomer.
  • the first step comprises cleaning the surface to remove the opacity and subsequently coating the cleaned surface to prevent further clouding.
  • a composition of a petroleum distillate emulsified in water is suitable.
  • the petroleum distillate is a mixture of hydrocarbons having a boiling point between 150°-190° C.; that is, the fraction in the distillation of petroleum between gasoline and the fuel oils as determined in accordance with Standard Method of Tests for Distillation of Gasoline, Naptha, Kerosene and Similar Petroleum Products (ASTM D 86).
  • the petroleum products found in this range are typically referred to as kerosene, coal oil, astrol oil or, more broadly, paraffinic mixtures of hydrocarbons as identified by their boiling point ranges.
  • paraffinic hydrocarbons may be applied directly in the cleaning step or may be emulsified with water of up to one part hydrocarbon to nine parts water by volume.
  • a pine oil-alcohol-water composition may be used such as Pine-Sol a product of American Cyanamid.
  • the coating composition comprises a polyester resin, such as an alkyd resin.
  • the alkyd resin is modified with an oil such as linseed, safflower, tung, and soy bean, and is further modified or copolymerized with monomers such as urethane, vinyl toluene, acrylic and/or vinyl monomers.
  • the resin is dissolved in a solvent such as petroleum distillates having a boiling point range of between 150° to 190° C. such as mineral spirits and optionally dryers are added which would be compatible with the formulation.
  • the dryers are any compatible oxidant which hastens the drying of the composition, such as a solution of lead, manganese or zinc salts of resin acids.
  • My invention will be described in reference to the cleaning and coating of surfaces of transparent acrylic windows, or sheets, the surfaces of which have become cloudy due to exposure to the sun.
  • a transparent acrylic sheet as commercially available is sold under the trademarks LUCITE or PLEXIGLAS, both well-known polymethylmethacrylates and products of DuPont and Rohm & Hass, respectively.
  • the cleaning step to clear the surfaces was accomplished as follows.
  • An aqueous emulsion of a petroleum distillate was used.
  • the petroleum distillate used is available commercially as kerosene. When emulsified in water, it is commercially sold under the trademark LESTOIL.
  • the cleaning solution was applied to the clouded surface by rubbing the mixture on the clouded surface, preferably using a circular motion. After rubbing for a predetermined time, between about 10 seconds to 1 minute, for example 30 seconds the surface was cleared and was subsequently wiped dry. At this point, the surface appeared to be transparent but the surface reclouded within an hour or more. Generally the clouded surface is the surface exposed directly to the sunlight. Depending upon the location and use of the sheet only one surface or both surfaces may have to be cleaned and coated.
  • the coating was applied by spraying it with a commercial sprayer preferably starting at the top of the sheet with the window standing in an upright position and allowing the material to drain down. The coating was continuously applied until no ripples appear and a uniform film is formed. The coating was then is allowed to air dry.
  • the coating is a hard clear gloss coating with excellent adhesion, abrasion resistance, good weathering, excellent chemical resistance and flexibility.
  • the oil modified-alkyd resins are combined with a monomer, for example, stryene, urethane, vinyl toluene, or acrylic monomers. Urethane alkyd is preferred.
  • LESTOIL For the cleaning solution, the commercial formulation of LESTOIL was used with varying amounts of water. More specifically, in parts by volume, LESTOIL/water the following ratios were found satisfactory: 1:0.5; 1:1; 1:2 and 1:3 to completely clear the surface.
  • PINE SOL having the formulation; Pine oil 30.0%; isopropanol 10.9%; soap 10%; and water 49.1% was used.
  • any solvent such as mineral spirits which would be a volatile component compatible with the formulation may be used.
  • mineral spirits having a bulking value of 6.50 lbs. per gallon the percent volatile by weight in the final formulation based on the addition of 12-20 fluid ozs. will range between about 71 to 78%. This is based on the additional between 12 and 20 fluid ozs. of solvent, such as mineral spirits to the commercially available formulations described above.
  • the dryers may be added optionally, as desired.
  • the formulations may be used alone to both clean and coat the surfaces.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Detergent Compositions (AREA)

Abstract

Clouded acrylate surfaces are cleaned permanently. The clouded surface is first cleaned using a petroleum distillate. Subsequently, a coating of an oil-monomer modified alkyl resin, 71-78% non-volatile, is coated on the surface to prevent further clouding.

Description

This application is a continuation of application Ser. No. 973,400, filed Dec. 26, 1978 now abandoned.
BACKGROUND AND BRIEF SUMMARY OF THE INVENTION
This invention relates to a method and composition for cleaning and preserving in a clear condition transparent plastic sheets for example, windows, such as "PLEXIGLAS".
U.S. Pat. Nos. 3,904,732 and 3,677,821 are broadly directed to restoring the surfaces of plastic sheets such as "LUCITE" and "PLEXIGLAS", polymethylmethacrylates.
My invention is more particularly directed to overcoming the problems associated with so-called plastic or synthetic transparent windows such as those windows formulated primarily or entirely from methylmethacrylate.
These windows after a period of time tend to cloud or become less transparent and therefore more opaque. In the cleaning of these windows with the use of commercial cleaners, two problems have been encountered: first, most commercial cleaners, such as are available to consumers at the retail level, will not remove the cloudiness or opaqueness from these windows; second, those few commercial cleaners available that will, in fact, clear the windows, such as "LESTOIL"®, a product of Noxell Corporation of Baltimore, Md., will only temporarily restore the transparency.
I have overcome the aforementioned problems of the inability to clean and maintain such windows in a clear or transparent condition by using a two-step process to clear permanently such windows. If the windows are initially clear, then only one of the two steps of my process and formulation is required.
Broadly, my invention comprises cleaning a surface of a transparent methylmethacrylate (a thermoplastic poly-type polymer more specifically an acrylic monomer). Where the acrylic surface is clouded, the first step comprises cleaning the surface to remove the opacity and subsequently coating the cleaned surface to prevent further clouding.
In the first step it has been found that a composition of a petroleum distillate emulsified in water is suitable. The petroleum distillate is a mixture of hydrocarbons having a boiling point between 150°-190° C.; that is, the fraction in the distillation of petroleum between gasoline and the fuel oils as determined in accordance with Standard Method of Tests for Distillation of Gasoline, Naptha, Kerosene and Similar Petroleum Products (ASTM D 86). The petroleum products found in this range are typically referred to as kerosene, coal oil, astrol oil or, more broadly, paraffinic mixtures of hydrocarbons as identified by their boiling point ranges. These paraffinic hydrocarbons may be applied directly in the cleaning step or may be emulsified with water of up to one part hydrocarbon to nine parts water by volume. Alternatively a pine oil-alcohol-water composition may be used such as Pine-Sol a product of American Cyanamid.
In the second step of the process, a coating composition is applied. The coating composition forms a film which permanently adheres to the surface and prevents further clouding. Also, it has been found that the formulations per se will clean the surface but not to the same degree of clearness (clarity) as the combination of both steps. Broadly, the coating composition comprises a polyester resin, such as an alkyd resin. The alkyd resin is modified with an oil such as linseed, safflower, tung, and soy bean, and is further modified or copolymerized with monomers such as urethane, vinyl toluene, acrylic and/or vinyl monomers. The resin is dissolved in a solvent such as petroleum distillates having a boiling point range of between 150° to 190° C. such as mineral spirits and optionally dryers are added which would be compatible with the formulation. The dryers are any compatible oxidant which hastens the drying of the composition, such as a solution of lead, manganese or zinc salts of resin acids.
DESCRIPTION OF THE PREFERRED EMBODIMENT
My invention will be described in reference to the cleaning and coating of surfaces of transparent acrylic windows, or sheets, the surfaces of which have become cloudy due to exposure to the sun.
A transparent acrylic sheet as commercially available is sold under the trademarks LUCITE or PLEXIGLAS, both well-known polymethylmethacrylates and products of DuPont and Rohm & Hass, respectively.
The surfaces of such sheets after a period of time, as is well known, tend to cloud or become opaque rendering the window less transparent. In order to clean permanently the sheet the following steps are effected.
In the following Examples the cleaning step to clear the surfaces was accomplished as follows. An aqueous emulsion of a petroleum distillate was used. The petroleum distillate used is available commercially as kerosene. When emulsified in water, it is commercially sold under the trademark LESTOIL. The cleaning solution was applied to the clouded surface by rubbing the mixture on the clouded surface, preferably using a circular motion. After rubbing for a predetermined time, between about 10 seconds to 1 minute, for example 30 seconds the surface was cleared and was subsequently wiped dry. At this point, the surface appeared to be transparent but the surface reclouded within an hour or more. Generally the clouded surface is the surface exposed directly to the sunlight. Depending upon the location and use of the sheet only one surface or both surfaces may have to be cleaned and coated.
In the following Examples, the coating was applied by spraying it with a commercial sprayer preferably starting at the top of the sheet with the window standing in an upright position and allowing the material to drain down. The coating was continuously applied until no ripples appear and a uniform film is formed. The coating was then is allowed to air dry.
The coating is a hard clear gloss coating with excellent adhesion, abrasion resistance, good weathering, excellent chemical resistance and flexibility. The oil modified-alkyd resins are combined with a monomer, for example, stryene, urethane, vinyl toluene, or acrylic monomers. Urethane alkyd is preferred.
For the cleaning solution, the commercial formulation of LESTOIL was used with varying amounts of water. More specifically, in parts by volume, LESTOIL/water the following ratios were found satisfactory: 1:0.5; 1:1; 1:2 and 1:3 to completely clear the surface.
Alternatively for the cleaning solution, PINE SOL having the formulation; Pine oil 30.0%; isopropanol 10.9%; soap 10%; and water 49.1% was used.
EXAMPLE I
U2 polyurethane-Clear Gloss as manufactured by Sterling Clark Lurton Corporation, Malden, Mass., having the formulation by weight percent linseed alkyd modified with toluene diisocyanate, 45% and mineral spirits and dryers 55% was used. To 32 fluid ozs. of this commercial coating was added 16 fluid ozs. of mineral spirits and 1 fluid oz. of dryers. The final formulation was applied to the cleaned surface before reclouding commenced, e.g., within 10 to 20 minutes. Three months after coating, the window remained transparent.
EXAMPLE II
A Polyurethane Varnish 012 Gloss Spar as manufactured by General Paint and Chemical Company, Division of Cotter & Company, Chicago, Ill., having the formulation by weight percent, non-volatile 41% (toluene dissocyanate soya copolymer), volatile 59% (mineral spirits 99%, dryers 1%) was used. To 32 fluid ozs. of this commercial coating as in Example I, was added 16 fluid ozs. of mineral spirits and 1 fluid oz. of dryers. A cleaned surface was coated with formulation before reclouding commenced. After three months the window was still transparent.
EXAMPLE III
70-28 (568) Semi-Gloss as manufactured by Dutchboy Paints, West Caldwell, N.J., having the formulation by weight percent, non-volatile (vinyl alkyd copolymer) 33.7% and volatile (mineral spirits) 66.3% was used. To 32 fluid ozs. of this commercial coating was added 16 fluid ozs of mineral spirits and 1.0 fluid oz. of dryers. A cleared surface was coated with this formulation. After three months the window was still transparent.
For all surfaces cleaned but not coated re-clouding commenced within one hour.
Although 16 fluid ozs. of mineral spirits was used, any solvent such as mineral spirits which would be a volatile component compatible with the formulation, may be used. Where mineral spirits are used having a bulking value of 6.50 lbs. per gallon the percent volatile by weight in the final formulation based on the addition of 12-20 fluid ozs. will range between about 71 to 78%. This is based on the additional between 12 and 20 fluid ozs. of solvent, such as mineral spirits to the commercially available formulations described above. The dryers may be added optionally, as desired.
Depending on the degree of clouding the formulations may be used alone to both clean and coat the surfaces.

Claims (7)

Having described my invention what I now claim is:
1. A method for cleaning and preventing clouding of transparent methylmethacrylate sheets which includes:
coating the surface of the sheet with a formulation which consists essentially of a non-volatile oil-monomer modified alkyd resin, the monomer selected from the group consisting of styrene, vinyl toluene, urethane and acrylic monomers; and a volatile solvent, the solvent being a petroleum distillate having a boiling point range between 150°-190° C., the non-volatile resin comprising 22-29% by weight of the formulation and the volume volatile solvent comprising 78-71% by weight of the formulation to form a clear film which prevents clouding of the acrylate sheet.
2. The method of claim 1 wherein the oil is selected from the group consisting of linseed, safflower, tung and soybean oils.
3. The method of claim 1 wherein the resin is linseed alkyd modified with toluene diisocyante.
4. The method of claim 1 wherein the resin is soya alkyd modified with toluene diisocyante.
5. The method of claim 1 wherein the resin is modified with a vinyl alkyd copolymer.
6. The method of claims 1, 2, 3, 4 or 5 which includes:
cleaning the acrylate surface with a petroleum distillate having a boiling point range of between 150°-180° prior to coating the surface.
7. The method of claims 1, 2, 3, 4 or 5 which includes:
cleaning the acrylate surface with a pine oil-alcohol-water formulation.
US06/331,489 1978-12-26 1981-12-17 Method for cleaning and clearing plastic surfaces Expired - Fee Related US4479985A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US06/331,489 US4479985A (en) 1978-12-26 1981-12-17 Method for cleaning and clearing plastic surfaces
US06/666,563 US4595719A (en) 1981-12-17 1984-10-30 Composition for cleaning and clearing plastic surfaces

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US97340078A 1978-12-26 1978-12-26
US06/331,489 US4479985A (en) 1978-12-26 1981-12-17 Method for cleaning and clearing plastic surfaces

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US97340078A Continuation 1978-12-26 1978-12-26

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US06/666,563 Division US4595719A (en) 1981-12-17 1984-10-30 Composition for cleaning and clearing plastic surfaces

Publications (1)

Publication Number Publication Date
US4479985A true US4479985A (en) 1984-10-30

Family

ID=26987786

Family Applications (1)

Application Number Title Priority Date Filing Date
US06/331,489 Expired - Fee Related US4479985A (en) 1978-12-26 1981-12-17 Method for cleaning and clearing plastic surfaces

Country Status (1)

Country Link
US (1) US4479985A (en)

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1643251A (en) * 1926-08-11 1927-09-20 George A Mcbride Composition for cleaning and polishing glass
US1764392A (en) * 1925-04-29 1930-06-17 Diebold Fritz Composition for cleaning glass windows
US1875552A (en) * 1929-10-28 1932-09-06 Goodyear Tire & Rubber Mold cleaning solution
US2713039A (en) * 1948-06-22 1955-07-12 American Cyanamid Co Modified alkyd resins and process of preparing same
US2862898A (en) * 1954-10-07 1958-12-02 Monsanto Chemcial Company Modified alkyd resins
US2967163A (en) * 1959-03-25 1961-01-03 Jacob M Fain Rain repellent composition comprising a styrenated oil modified alkyd resin with paraffin wax
US2986543A (en) * 1958-10-20 1961-05-30 American Cyanamid Co Process for preparing styrenated nondrying and/or semi-drying oil modified alkyd resins by incremental monomeric addition
US3382294A (en) * 1963-05-03 1968-05-07 Pittsburgh Plate Glass Co Coating composition comprising an acrylic inter-polymer, an amine-aldehyde resin, and an alkyd resin
US3501425A (en) * 1964-07-30 1970-03-17 Reichhold Chemicals Inc Process for preparing thixotropic solutions of oil-modified alkyd resins and resulting product
US3515579A (en) * 1968-06-21 1970-06-02 Nat Patent Dev Corp Non-fogging transparent material
US3677821A (en) * 1967-12-29 1972-07-18 Lion Fat Oil Co Ltd Method for reconditioning the surface of plastics
US3876575A (en) * 1970-07-22 1975-04-08 Nippon Oil Co Ltd Process for producing resins of weather resistance
US3904732A (en) * 1974-10-22 1975-09-09 Us Army Method for improving transparency of thermally damaged acrylic glazing

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1764392A (en) * 1925-04-29 1930-06-17 Diebold Fritz Composition for cleaning glass windows
US1643251A (en) * 1926-08-11 1927-09-20 George A Mcbride Composition for cleaning and polishing glass
US1875552A (en) * 1929-10-28 1932-09-06 Goodyear Tire & Rubber Mold cleaning solution
US2713039A (en) * 1948-06-22 1955-07-12 American Cyanamid Co Modified alkyd resins and process of preparing same
US2862898A (en) * 1954-10-07 1958-12-02 Monsanto Chemcial Company Modified alkyd resins
US2986543A (en) * 1958-10-20 1961-05-30 American Cyanamid Co Process for preparing styrenated nondrying and/or semi-drying oil modified alkyd resins by incremental monomeric addition
US2967163A (en) * 1959-03-25 1961-01-03 Jacob M Fain Rain repellent composition comprising a styrenated oil modified alkyd resin with paraffin wax
US3382294A (en) * 1963-05-03 1968-05-07 Pittsburgh Plate Glass Co Coating composition comprising an acrylic inter-polymer, an amine-aldehyde resin, and an alkyd resin
US3501425A (en) * 1964-07-30 1970-03-17 Reichhold Chemicals Inc Process for preparing thixotropic solutions of oil-modified alkyd resins and resulting product
US3677821A (en) * 1967-12-29 1972-07-18 Lion Fat Oil Co Ltd Method for reconditioning the surface of plastics
US3515579A (en) * 1968-06-21 1970-06-02 Nat Patent Dev Corp Non-fogging transparent material
US3876575A (en) * 1970-07-22 1975-04-08 Nippon Oil Co Ltd Process for producing resins of weather resistance
US3904732A (en) * 1974-10-22 1975-09-09 Us Army Method for improving transparency of thermally damaged acrylic glazing

Similar Documents

Publication Publication Date Title
US5700522A (en) Aqueous emulsion-based coating compositions
CA1201544A (en) Water based thickened stain
US6033736A (en) Aqueous wax emulsion as paint primer and paint repair adhesive
US5631042A (en) Graffiti-resistant barriers, related compositions and methods24m
US5330787A (en) Polish composition forming hydrophilic layer and spray-away polishing process
US7638165B2 (en) Method of treating a surface, coating compositions and use thereof and coated surfaces obtainable by the use
SE459812B (en) AEROSOLPHERIC COMPOSITION INCLUDING TWO MOVIE PHOTOGRAPHY POLYMER BINDING AGENTS
Hamburg Hess’s Paint Film Defects: Their Causes and Cure
US7074262B2 (en) Silicone compositions for use in tire dressing and methods of making
US3776752A (en) Process for finishing surfaces
CA1311869C (en) Waterborne pigmented acrylic hydrosol coating composition and process
Gooch Lead-based paint handbook
US2860074A (en) Vevyl resin-acrylic ester-organopoly-
US4479985A (en) Method for cleaning and clearing plastic surfaces
US4595719A (en) Composition for cleaning and clearing plastic surfaces
AU2266292A (en) Aqueous emulsion-based coating compositions
Roberts Organic coatings; properties, selection, and use
JPH0613663B2 (en) Coating treatment agent for painted surface
US5565516A (en) Finishing compositions
US2346622A (en) Remover for paint, varnish, and the like
Collier Wood Finishing: Pergamon Series of Monographs on Furniture and Timber
US2479762A (en) Corrosion preventing composition
JPH06264004A (en) Lowly odoriferous aerosol coating material composition
Pomerantz et al. Conservators advise artists
US2517904A (en) Self-polishing wax composition

Legal Events

Date Code Title Description
FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
FP Lapsed due to failure to pay maintenance fee

Effective date: 19921101

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362